Taiwan FDA registration 8bbe8ca976753b6268d0d17f18769136
"Chongjin" respiratory tract (unsterilized)
TW: "崇仁" 呼吸器管路 (未滅菌)
Taiwan·Risk Class 1·GALEMED (XIAMEN) CO., LTD.·Registered Dec 27, 2019 – Dec 27, 2024ExpiredRegistration details
- Analysis ID
- 8bbe8ca976753b6268d0d17f18769136
- Customs Code
- DHA09600405903
Company information
- Manufacturer
- GALEMED (XIAMEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GALEMED CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 27, 2019
- Expiry Date
- Dec 27, 2024
About this record
Access comprehensive regulatory information for "Chongjin" respiratory tract (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8bbe8ca976753b6268d0d17f18769136 and manufactured by GALEMED (XIAMEN) CO., LTD.. The authorized representative in Taiwan is GALEMED CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices